View drug registration information details.
| Items | Registration information |
|---|
| ID | 561 |
|---|
| No | 561 |
|---|
| Brand Name | RECORMON 4,000 IU |
|---|
| Ingredients | EPOETIN BETA 4,000 IU/0.3ML |
|---|
| Dosage Form | SOLUTION FOR INJECTION |
|---|
| Primary Packaging | syringe |
|---|
| Storage | |
|---|
| Shelf Life | 2 YEARS |
|---|
| Pack Size | BOX OF 6 PRE-FILLED SYRINGES WITH NEEDLES 27 G1/12 |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | TREATMENT OF: RENAL ANEMIA, SYMPTOMATIC ANEMIA IN CANCER PATIENTS. - PREVENTION OF ANEMIA OF PREMATURITY. - TREATMENT FOR INCREASING THE AMOUNT OF AUTOLOGOUS BLOOD |
|---|
| Contraindications | |
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| Side Effects | |
|---|
| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | COLOURLESS, CLEAR SOLUTION |
|---|
| Note | |
|---|
| License Owner | DKSH LAOS COMPANY LIMITED |
|---|
| Manufacturer | ROCHE DIAGNOSTICS GMBH |
|---|
| Country | GERMANY |
|---|
| Import Registration No | |
|---|
| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 09 I 2082/01 |
|---|
| FDD Registration Date | 31-Mar-2023 |
|---|
| Expiry Date | 30-Mar-2026 |
|---|
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